Canonical Allele Identifier: PA103139
Gene: TPP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000382.3:p.Cys365Arg
CA252376
NM_000391.4:c.1093T>C